An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. [electronic resource]
Producer: 20080102Description: 18537-42 p. digitalISSN:- 1091-6490
- Animals
- Animals, Newborn
- Calcium -- metabolism
- Embryo, Mammalian -- embryology
- Fetal Growth Retardation -- genetics
- Gene Expression Regulation, Developmental
- Heart -- embryology
- Homozygote
- Isoleucine -- genetics
- Mice
- Mice, Transgenic
- Microscopy, Electron
- Muscle Fibers, Skeletal -- metabolism
- Muscle, Skeletal -- embryology
- Mutation -- genetics
- Ryanodine Receptor Calcium Release Channel -- genetics
- Skeleton
- Threonine -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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